HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(2-Hexylsulfanyl-6-methyl-pyrimidin-4-yl)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Hydroxy-3-hexyn-2-one | HCID 10898675 | — |
| Reactant | (Hexylsulfanyl)methanimidamide hydrobromide | HCID 12387367 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Hexylsulfanyl-6-methyl-pyrimidin-4-yl)-ethanol | HCID 69290720 | 61.1% |
Reaction Steps
5-Hydroxy-hex-3-yn-2-one (2 g, 18 mmol) and 2-hexyl-isothiourea hydrobromide (5.2 g, 21 mmol) were dissolved in THF (10 mL). Then the triethylamine (5.5 mL, 40 mmol) was added and stirring continued for 3 h. The reaction was slightly exothermic. The mixture was extracted with AcOEt and sat. NH4Cl solution. The crude product was purified by chromatography on silica gel with a heptane/AcOEt gradient. One obtained 2.8 g (61%) of a light yellow oil. MS: m/z=254 (M)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351700B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-ed720e50adf24ada9468f6f2da1ed40f |
| Source note | uspto-grants-2008_04 |